A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5499n100



Internal ID20157115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187514678..188139456hg38UCSC Ensembl
chr4:188435832..189060610hg19UCSC Ensembl
chr4:188672826..189297604hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38624779
hg19624779
hg18624779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022112, nsv1025971, nsv1027384, nsv1025366, nsv1026487
Samples
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5499n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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